Introduction
FAS-II System
Mechanism of Action
General Structural Information
Crystal structures of InhA reveal a (each subunit featured with a different color) in aqueous solution with separate ligand binding sites in each subunit. Each subunit is composed of 289 residues and features a typical
Rossmann fold containing a single NADH binding site. The of InhA is made up of several alpha helices (pink), beta sheets (gold), and beta turns (white). This enzyme also features a fatty acyl binding crevice that accommodates the long-chain fatty acyl substrate needed to synthesize mycolic acid precursors. The of the InhA form one side of the fatty acyl binding crevice, referred to as the (residues 196-219).
Fatty Acyl Binding Crevice (substrate binding loop in purple; substrates pictured inside the crevice)
One side of this crevice is open and exposed to solvent, which allows the substrates to access the binding pocket of this enzyme. The size of the substrate binding loop is a primary determinant of the ability of InhA to select for fatty acyl chains longer than 16 carbons to successfully produce mycolic acid precursors.
Talk generally about catalytic triad. More specific details in sections below.
Fatty Acyl Binding Crevice
Within the fatty acyl binding crevice, the NADH substrate sits on the top shelf of the Rossmann fold, and the fatty acyl substrate sits on top of the NADH substrate. Both of these substrates are held in place through interactions with the side chains of (purple) residues.
Substrate Binding Pocket (NADH in green; fatty acyl substrate in red)
The majority of these residues anchoring the substrates are found within the substrate binding loop itself, including Ala-198, Met-199, Ala-201, Ile-202, Leu-207, Ile-215, and Leu-218. Studies have found that the fatty acyl substrate adopts a u-shaped conformation to facilitate binding.
Catalytic Triad
Hydrogen Bonding Interactions
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Clinical Applications
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